Canonical Allele Identifier: PA110010
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Gly357Glu
CA255437
NM_000133.4:c.1070G>A